Dimethyl (1-hydr­oxy-1,2-diphenyl­ethyl)phospho­nate

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In the mol­ecule of the title compound, C(16)H(19)O(4)P, the coordination around the P atom is distorted tetra­hedral. The aromatic rings are oriented at a dihedral angle of 72.28 (11)°. Intra­molecular C—H⋯O hydrogen bonding result in the formation of five- and six-membered rings. In the crystal st...

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Autores principales: Acar, Nurcan, Tahir, M. Nawaz, Yılmaz, Hamza, Chishti, Muhammad Saeed Ahmad, Malik, Muhammad Ali
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968507/
https://www.ncbi.nlm.nih.gov/pubmed/21582150
http://dx.doi.org/10.1107/S1600536809004036
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author Acar, Nurcan
Tahir, M. Nawaz
Yılmaz, Hamza
Chishti, Muhammad Saeed Ahmad
Malik, Muhammad Ali
author_facet Acar, Nurcan
Tahir, M. Nawaz
Yılmaz, Hamza
Chishti, Muhammad Saeed Ahmad
Malik, Muhammad Ali
author_sort Acar, Nurcan
collection PubMed
description In the mol­ecule of the title compound, C(16)H(19)O(4)P, the coordination around the P atom is distorted tetra­hedral. The aromatic rings are oriented at a dihedral angle of 72.28 (11)°. Intra­molecular C—H⋯O hydrogen bonding result in the formation of five- and six-membered rings. In the crystal structure, inter­molecular C—H⋯O hydrogen bonds link the mol­ecules. There is also a weak C—H⋯π inter­action.
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spelling pubmed-29685072010-12-30 Dimethyl (1-hydr­oxy-1,2-diphenyl­ethyl)phospho­nate Acar, Nurcan Tahir, M. Nawaz Yılmaz, Hamza Chishti, Muhammad Saeed Ahmad Malik, Muhammad Ali Acta Crystallogr Sect E Struct Rep Online Organic Papers In the mol­ecule of the title compound, C(16)H(19)O(4)P, the coordination around the P atom is distorted tetra­hedral. The aromatic rings are oriented at a dihedral angle of 72.28 (11)°. Intra­molecular C—H⋯O hydrogen bonding result in the formation of five- and six-membered rings. In the crystal structure, inter­molecular C—H⋯O hydrogen bonds link the mol­ecules. There is also a weak C—H⋯π inter­action. International Union of Crystallography 2009-02-06 /pmc/articles/PMC2968507/ /pubmed/21582150 http://dx.doi.org/10.1107/S1600536809004036 Text en © Acar et al. 2009 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Acar, Nurcan
Tahir, M. Nawaz
Yılmaz, Hamza
Chishti, Muhammad Saeed Ahmad
Malik, Muhammad Ali
Dimethyl (1-hydr­oxy-1,2-diphenyl­ethyl)phospho­nate
title Dimethyl (1-hydr­oxy-1,2-diphenyl­ethyl)phospho­nate
title_full Dimethyl (1-hydr­oxy-1,2-diphenyl­ethyl)phospho­nate
title_fullStr Dimethyl (1-hydr­oxy-1,2-diphenyl­ethyl)phospho­nate
title_full_unstemmed Dimethyl (1-hydr­oxy-1,2-diphenyl­ethyl)phospho­nate
title_short Dimethyl (1-hydr­oxy-1,2-diphenyl­ethyl)phospho­nate
title_sort dimethyl (1-hydr­oxy-1,2-diphenyl­ethyl)phospho­nate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968507/
https://www.ncbi.nlm.nih.gov/pubmed/21582150
http://dx.doi.org/10.1107/S1600536809004036
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AT tahirmnawaz dimethyl1hydroxy12diphenylethylphosphonate
AT yılmazhamza dimethyl1hydroxy12diphenylethylphosphonate
AT chishtimuhammadsaeedahmad dimethyl1hydroxy12diphenylethylphosphonate
AT malikmuhammadali dimethyl1hydroxy12diphenylethylphosphonate

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